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231.
232.
A generalized Schrödinger formalism has been presented which is obtained as a Hilbert space representation of a Liouville equation generalized to include the action as a dynamical variable, in addition to the positions and the momenta. This formalism applied to a classical mechanical system had been shown to yield a similar set of Schrödinger like equations for the classical dynamical system of charged particles in a magnetic field. The novel quantum-like predictions for this classical mechanical system have been experimentally demonstrated and the results are presented. 相似文献
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236.
R. Ramani P. Ramachandra T. S. G. Ravichandran G. Ramagopal S. Gopal C. Ranganathaiah 《Applied Physics A: Materials Science & Processing》1995,60(5):481-486
Positron Annihilation Lifetime Spectroscopy (PALS) is used to probe the micro-structural changes in the polymer polycarbonate in terms of the changes in free volume hole size and their content as a function of temperature. The measured spectra are best fitted to three lifetime component analysis. The average hole size in the amorphous regions is determined from the measured Ortho Positronium (O-Ps) lifetime 3 by following the treatment of Nakanishi et al. On the other hand, information about defects in the crystalline regions is revealed by trapped positrons lifetime 2. In this polymer the average hole radius varies from 2.71 Å to 2.77 Å. The present study indicates that this polymer has a glass transition temperature of 152°C. Further, we have calculated the trapping rates in the ordered and disordered regions of the polymer based on Goldanskii's kinetic equations and an attempt is made for the first time to estimate the activation energy in the amorphous and crystalline regions separately. 相似文献
237.
Linda L. Maggiora James D. Petke Dama Gopal Reynold T. Iwamoto Gerald M. Maggiora 《Photochemistry and photobiology》1985,42(1):69-75
Abstract— A protonated Schiff base of Ni (II)-pyrochlorophyll a has been synthesized which exhibits a reversible bathochromic shift of 504 cm-1 relative to Ni (II)-pyrochlorophyll a. The magnitude of this shift lies between those observed for P700 and P680, the photoactive pigments of photosystems I and II in plants. Cyclic voltammetric measurements show that the protonated Schiff base is about 0.2 V more difficult to oxidize than its unprotonated form. These results suggest that a protonated Schiff base may be a better model for P680 than, as was originally assumed, for P700. In addition, the results of solvent and counterion effect studies show that microenvironmental perturbations in the neighborhood of the protonated Schiff base moiety are unlikely to induce further spectral shifts. Ab initio quantum mechanical calculations show a small hypsochromic shift rather than the observed bathochromic one, and the reasons for this discrepancy are discussed. 相似文献
238.
Oxidation of 2-hydroxy-3-nitrochalcones with thallium(III) nitrate gives (Z)-2-phenylmethylene-7-nitrobenzofuran-3(2H)-one derivatives, rather than the more usual 1,2-diaryl-3,3-dimethoxypropan-1-ones or the corresponding isoflavones.
Oxydative Cyclisierung von Chalconen mit Thallium(III)nitrat: Synthese von (Z)-2-Phenylmethylen-7-nitro-3(2H)-benzofuranonen (Kurze Mitteilung)
Zusammenfassung Die Oxidation von 2-Hydroxy-3-nitrochalconen mit Thallium(III)nitrat ergab (Z)-2-Phenylmethylen-7-nitro-3(2H)-benzofuranon-Derivate und nicht die üblichen 1,2-Diaryl-3,3-dimethoxypropan-1-one bzw. die entsprechenden Isoflavone.相似文献
239.
The bromination reaction of azo compounds with N-bromosuccinimide in acetic acid medium has been studied. Some reaction products have been isolated and reaction mechanisms suggested. The reaction study has been applied for the determination of 2-10 mg of azo compounds. The maximum deviation of the results from the theoretical value is generally within +/- 1%. 相似文献
240.
I. K. Varma R. N. Goel D. S. Varma 《Journal of polymer science. Part A, Polymer chemistry》1979,17(3):703-713
Polyimides with different proportions of m-phenylene and p-phenylene (or p,p′-biphenylene) were prepared by polymerizing different molar ratios of m-phenylene diamine and p-phenylene diamine (or p,p′-diaminobiphenyl) with pyromellitic dianhydride in dimethylformamide at 0°C. Chemical cyclodehydration of polyamic acids resulted in the corresponding polyimides. Polymers were characterized by infrared (IR), viscosity, and density measurements. Viscosity and density of polymers decreased with an increase on m-phenylene groups in the backbone. The thermal and thermooxidative stabilities were investigated by dynamic thermogravimetry. Stability decreased when m-phenylene groups were introduced in the backbone. 相似文献